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(S)-3-Amino-4-(3-thienyl)butanoic acid hydrochloride is a chemical compound that belongs to the class of organic compounds known as L-alpha-amino acids. It is characterized by a carboxylic acid functional group located at the alpha carbon and an amino group. (S)-3-Amino-4-(3-thienyl)butanoic acid hydrochloride features a thiophene ring, which contributes to its chemical reactivity and distinctive properties. The "S" in its name indicates the configuration of its chiral center, and the presence of a hydrochloric acid component, which often enhances the compound's solubility and stability.

270262-99-2

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270262-99-2 Usage

Uses

Used in Pharmaceutical Applications:
(S)-3-Amino-4-(3-thienyl)butanoic acid hydrochloride is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structural features, including the thiophene ring and the L-alpha-amino acid configuration, make it a valuable building block for the development of new drugs.
Used in Research Applications:
In the field of research, (S)-3-Amino-4-(3-thienyl)butanoic acid hydrochloride is used as a reagent for studying the properties and reactivity of L-alpha-amino acids and their derivatives. Its presence in the compound allows researchers to investigate the effects of the thiophene ring on the compound's chemical behavior and interactions with other molecules.
Used in Chemical Synthesis:
(S)-3-Amino-4-(3-thienyl)butanoic acid hydrochloride is used as a starting material in the synthesis of various organic compounds. Its unique structure and reactivity make it a useful component in the preparation of complex molecules, such as pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Analytical Chemistry:
(S)-3-Amino-4-(3-thienyl)butanoic acid hydrochloride can be used as a reference compound in analytical chemistry for the determination of the properties of L-alpha-amino acids and their derivatives. Its distinctive features, such as the thiophene ring and the hydrochloride component, can be used to calibrate analytical instruments and develop new methods for the analysis of similar compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 270262-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,2,6 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 270262-99:
(8*2)+(7*7)+(6*0)+(5*2)+(4*6)+(3*2)+(2*9)+(1*9)=132
132 % 10 = 2
So 270262-99-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO2S.ClH/c9-7(4-8(10)11)3-6-1-2-12-5-6;/h1-2,5,7H,3-4,9H2,(H,10,11);1H/t7-;/m0./s1

270262-99-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-AMINO-4-(3-THIENYL)BUTANOIC ACID HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:270262-99-2 SDS

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